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Year | Number of Results |
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Page 1
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.
Nat Genet. 2012 Oct;44(10):1080-3. doi: 10.1038/ng.2406. Epub 2012 Sep 9.
Nat Genet. 2012.
PMID: 22961002
A Suzuki-type multivalued contraction on weak partial metric spaces and applications.
Aydi H, Barakat MA, Mitrović ZD, Šešum-Čavić V.
Aydi H, et al. Among authors: mitrovic zd.
J Inequal Appl. 2018;2018(1):270. doi: 10.1186/s13660-018-1866-9. Epub 2018 Oct 5.
J Inequal Appl. 2018.
PMID: 30363760
Free PMC article.
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Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.
Evgrafov OV, Mersiyanova I, Irobi J, Van Den Bosch L, Dierick I, Leung CL, Schagina O, Verpoorten N, Van Impe K, Fedotov V, Dadali E, Auer-Grumbach M, Windpassinger C, Wagner K, Mitrovic Z, Hilton-Jones D, Talbot K, Martin JJ, Vasserman N, Tverskaya S, Polyakov A, Liem RK, Gettemans J, Robberecht W, De Jonghe P, Timmerman V.
Evgrafov OV, et al. Among authors: mitrovic z.
Nat Genet. 2004 Jun;36(6):602-6. doi: 10.1038/ng1354. Epub 2004 May 2.
Nat Genet. 2004.
PMID: 15122254
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Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNA(Trp) gene.
Barić I, Fumić K, Petković Ramadža D, Sperl W, Zimmermann FA, Muačević-Katanec D, Mitrović Z, Pažanin L, Cvitanović Šojat L, Kekez T, Reiner Z, Mayr JA.
Barić I, et al. Among authors: mitrovic z.
Eur J Hum Genet. 2013 Aug;21(8):871-5. doi: 10.1038/ejhg.2012.272. Epub 2012 Dec 12.
Eur J Hum Genet. 2013.
PMID: 23232693
Free PMC article.
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Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study.
Dierick I, Baets J, Irobi J, Jacobs A, De Vriendt E, Deconinck T, Merlini L, Van den Bergh P, Rasic VM, Robberecht W, Fischer D, Morales RJ, Mitrovic Z, Seeman P, Mazanec R, Kochanski A, Jordanova A, Auer-Grumbach M, Helderman-van den Enden AT, Wokke JH, Nelis E, De Jonghe P, Timmerman V.
Dierick I, et al. Among authors: mitrovic z.
Brain. 2008 May;131(Pt 5):1217-27. doi: 10.1093/brain/awn029. Epub 2008 Mar 5.
Brain. 2008.
PMID: 18325928
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Early-onset ataxia with progressive external ophthalmoplegia associated with POLG mutation: autosomal recessive mitochondrial ataxic syndrome or SANDO?
Habek M, Barun B, Adamec I, Mitrović Z, Ozretić D, Brinar VV.
Habek M, et al. Among authors: mitrovic z.
Neurologist. 2012 Sep;18(5):287-9. doi: 10.1097/NRL.0b013e318266f5a6.
Neurologist. 2012.
PMID: 22931735
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